ClinLab Staffing
Job Location :
Baltimore,MD, USA
Posted on :
2025-02-27T07:38:51Z
Job Description :
Responsibilities:
- Complete and maintain aseptic qualification training.
- Obtain basic understanding of a task, unit operation and/or document (forms and/or SOPs) while aiding with oversight from Manufacturing Technician III and above.
- Attain and maintain gowning qualification per appropriate SOPs.
- Follow SOPs, product batch record instructions, logbooks and forms, and corresponding quality documentation in detail.
- Prepare and maintain accurate documentation following cGMP and GDP principles.
- Ensure documentations are completed in real-time in accordance to CGMP and GDP principles.
- Adhere to all environmental, health, and safety policies and procedures and proactively identify unsafe conditions.
- Support QC sampling, equipment calibration, equipment/utility validation, and preventive maintenance as needed.
- Work collaboratively with internal teams to meet site goals and objectives as part of a team.
- Initiate and foster a spirit of cooperation within and between departments.
- Review documentation for accuracy, makes corrections and/or escalates to supervision/Manufacturing Quality Associate (MQA).
- Maintain all personal cGMP related training in a current state.
- Achieve and maintain cleaning and sanitization of cleanroom training.
- Participate in Aseptic media qualification per the appropriate qualification protocol.
- Support manufacturing in the investigation of deviations and performs required risk assessments.
- Participate in personnel monitoring as requested.
- Work closely with Operational Excellence to identify and implement process improvements.
- Set up and breakdown the filling equipment per appropriate SOPs.
- Transport equipment and components as needed.
- Interact with filling machines at the validated speeds and volumes.
- Perform volume checks.
- Perform and document inherent and non-inherent interventions.
- Ensure slow and purposeful movements appropriate for a Grade A/B GMP aseptic environment.
- Work with R&D and tech transfer team for successful transfer of Programs into the GMP area
- Perform all aseptic connections, respecting first air.
- Perform pre- and post-filter integrity testing as required.
- Aseptically sterile filter products into appropriate vessels.
- Complete routine and enhanced cleaning and sanitization of all controlled aseptic cleanrooms, as needed.
- Attain and maintain ability to perform environmental tasks as required.
- Perform other duties as assigned.
Qualifications:
- High school diploma or equivalent with 1-3 years' experience, Bachelor's degree with a minimum of 1 year of experience, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities.
- Senior Manufacturing Technician (minimum of 3 years of industry experience w/ fill finish experience)
- Prior experience in related field, preferred.
- cGMP manufacturing knowledge, preferred.
- Aseptic filling and general production knowledge, preferred.
- Demonstrate basic math skills.
- Demonstrate the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates.
- Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision.
- Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required.
- Must be able to comprehend and follow all applicable SOPs.
- Demonstrate knowledge and experience with electronic Quality Management Systems such as MasterControl and Trackwise.
- Demonstrate ability to acquire the appropriate knowledge from resources on the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products.
- Good understanding of cGMPs, industry, and regulatory standards and guidelines.
- Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc.
- Demonstrate the ability to portray the appropriate level of integrity and professionalism.
- Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats.
- Demonstrate the ability to complete tasks accurately and according to established and shifting timelines.
- Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions.
- Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment.
- Results-oriented and efficient.
- Creative and open-minded who fosters an environment in which sharing of ideas is encouraged.
- Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally).
- Demonstrate the ability to work well in a cross-functional team environment.
- Must communicate fluently in English and have legible handwriting.
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